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Communication | Regular issue | Vol 53, No. 10, 2000, pp.2119-2122
Published online, 1st January, 1970
DOI: 10.3987/COM-00-8992
New Synthesis of KT5823 Indolocarbazole Aglycone

Guillaume E. Burtin,* Daivd J. Madge,* and David L. Selwood

*The Wolfson Institute for Biomedicinal Reseach, Biological and Medicinal Chemsitry, University College London, Cruciform Building, Gower Street, London, WC1E 6AU, U.K.

Abstract

The indolo[2,3-a]pyrrolo[3,4-c]carbazole aglycone of the selective protein kinase G inhibitor KT5823 has been synthesised in four steps and 36% overall yield from 2,3-dichloro-N-methylmaleimide by utilising an efficient new two step reduction sequence for the key imide to amide transformation.